MAUDE report
MAUDE report 42921: SIMS ARTERIAL BLOOD SAMPLE SYRINGE
Malfunction · received Oct 18, 1996 · SIMS SMITHS INDUSTRIES MEDICAL SYSTEMS
Key facts
| MDR report key | 42921 |
|---|---|
| Report number | 42921 |
| Event type | Malfunction |
| Brand name | SIMS ARTERIAL BLOOD SAMPLE SYRINGE |
| Model number | ALL |
| Catalog number | * |
| Manufacturer | SIMS SMITHS INDUSTRIES MEDICAL SYSTEMS |
| Product code | CBT |
| Device class | Class I |
| PMA or 510(k) number | Device Exempt |
| Date received by FDA | Oct 18, 1996 |
| Report date | Sep 30, 1996 |
| Report source | Maude |
At a glance
- None Device problems coded
- No Adverse event flagged
- Yes Product problem flagged
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About MAUDE medical device reports
MAUDE holds medical device reports (MDRs) of suspected device-associated deaths, serious injuries and malfunctions submitted to the FDA by manufacturers, importers, user facilities and the public. A report alone does not establish that a device caused an event.
Source: U.S. Food and Drug Administration (FDA), MAUDE (Manufacturer and User Facility Device Experience) database · Source date: